PARP Universal Colorimetric Assay Kit

Transcription

1 PARP Universal Colorimetric Assay Kit Catalog Number K 96-well colorimetric assay for screening Poly(ADP-ribose) Polymerase (PARP) inhibitors and quantitation of PARP activity in cells and tissue. This package insert must be read in its entirety before using this product. FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES.

2 Contents TABLE OF CONTENTS Page INTRODUCTION 2 PRINCIPLE OF THE ASSAY... 2 REAGENTS PROVIDED 3 MATERIALS REQUIRED BUT NOT PROVIDED... 3 PRECAUTIONS 3 LIMITATIONS OF THE PROCEDURE... 4 PREPARATION OF REAGENTS 4 PARP INHIBITOR SCREENING ASSAY PROTOCOL... 5 PARP ACTIVITY IN CELLS AND TISSUES 6 DATA INTERPRETATION... 8 TROUBLESHOOTING GUIDE 9 APPENDIX REFERENCES 10 MANUFACTURED FOR AND DISTRIBUTED BY: R&D Systems, Inc. TELEPHONE: (800) McKinley Place NE (612) Minneapolis, MN FAX: (612) United States of America info@rndsystems.com R&D Systems Europe, Ltd. 19 Barton Lane Abingdon Science Park TELEPHONE: +44 (0) Abingdon, OX14 3NB FAX: +44 (0) United Kingdom info@rndsystems.co.uk R&D Systems GmbH Borsigstrasse 7 TELEPHONE: +49 (0) Wiesbaden-Nordenstadt FAX: +49 (0) Germany infogmbh@rndsystems.co.uk R&D Systems Europe 77 boulevard Vauban FREEPHONE: LILLE CEDEX FAX: France info@rndsystems.co.uk

3 INTRODUCTION Poly (ADP-ribosylation) of nuclear proteins is a post-translational event that occurs in response to DNA damage. Poly (ADP-ribose) Polymerase (PARP) is the enzyme catalyzing the NAD-dependent addition of ribose to adjacent nuclear proteins. PARP is an abundant nuclear protein present in all somatic cells. PARP plays an important role in DNA repair but can also lead to cell death by depleting the cellular NAD pool (1-2). PARP is activated when it becomes attached to regions of damaged DNA. The enzyme catalyzes its own ADP-ribosylation at glutamic acid residues and to a lesser extent nuclear proteins such as histones. Automodification of PARP aids in the release of PARP from DNA, permitting access by repair enzymes to the sites of DNA damage. During apoptosis, PARP is specifically cleaved by members of the ICE family of proteases (e.g. Caspase-3). It is converted to an 85 kda fragment with minimal activity that is not activated by damaged DNA. It apppears that PARP cleavage is a mechanism that prevents apoptotic cells from repairing their DNA. Experiments have shown that PARP inhibition prevents tissue damage in animal models of myocardial and neuronal ischemia, diabetes, septic shock, and vascular stroke (3-10). Recent data implicate a synergistic function of Ku80 and PARP-1 in minimizing chromosome aberrations and cancer development (8). PRINCIPLE OF THE ASSAY The PARP Universal Colorimetric Assay Kit measures the incorporation of biotinylated Poly (ADP-ribose) onto histone proteins in a 96-well plate. This assay is ideal for the screening of PARP inhibitors and for measuring the activity of PARP in cells and tissue. Important features of the assay include a colorimetric, non-radioactive format, higher throughput 96 test size, and sensitivity down to 0.01 units of PARP per well. 2

4 REAGENTS PROVIDED Part Number Component Amount Provided Storage Aminobenzamide* 60 µl -80 C PARP-HSA Enzyme 50 µl -80 C X PARP Buffer* 500 µl -80 C X PARP Cocktail* 300 µl -80 C X Activated DNA* 300 µl -80 C X Strep-Diluent 2 ml 2-8 C P Histone-Coated Plate* 12 strips of 8 wells 2-8 C Strep-HRP 30 µl 2-8 C TACS-Sapphire 10 ml 2-8 C *These components can be stored at -20 C in a manual defrost freezer for up to 1 year, provided it is within the expiration date of the kit. Contains biotinylated NAD. MATERIALS REQUIRED BUT NOT PROVIDED Reagents Inhibitors or cells/tissue to be tested 1X PBS, ph 7.4 (without Ca 2+ or Mg 2+ ) Deionized or distilled water 1X PBS + 0.1% Triton X N HCl or 5% Phosphoric acid Phenylmethylsulfonyl fluoride (PMSF) and other protease inhibitors Triton X-100 or NP-40 and 1 M NaCl (for cell extract preparation) Detergent compatible protein determination reagents (i.e. Bradford or BCA) Disposables Pipette tips (1-200 L, L) 1.5 ml microtubes 15 ml centrifuge tubes Equipment Micropipettes Centrifuge Multi-channel pipette (1-50 L) Microplate washer (optional) Ice bath 96 well plate reader (630 nm or 450 nm filter) PRECAUTIONS The physical, chemical, and toxicological properties of the chemicals and reagents in this kit may not yet have been fully investigated. The use of gloves, lab coats, and eye protection is recommended. Material Safety Data Sheets are available upon request. 3

5 LIMITATIONS OF THE PROCEDURE FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES. The kit should not be used beyond the expiration date on the kit label. Do not mix or substitute reagents with those from other lots or sources. Any variation in operator, pipetting technique, washing technique, incubation time or temperature, and kit age can alter the performance of the assay. PREPARATION OF REAGENTS Refer to the Appendix on page 9 for additional reagent composition information. 1. 1X Strep-Diluent Dilute the 10X Strep-Diluent to 1X (1:10) in 1X PBS + 0.1% Triton X-100 before use. This solution is used as a diluent for the Strep-HRP. 2. 1X PARP Buffer Dilute the 20X PARP Buffer to 1X (1:20) with deionized or distilled water. The 1X PARP Buffer is used to dilute the PARP-HSA Enzyme, PARP Cocktail, the inhibitors to be tested (if required), and to prepare cell and tissue extracts. 3. 1X PARP Cocktail Dilute the 10X PARP Cocktail to 1X as follows. 10X PARP Cocktail 10X Activated DNA 1X PARP Buffer 2.5 L/well 2.5 L/well 20 L/well 4. PARP-HSA Enzyme This kit contains 50 L of PARP-HSA Enzyme at a concentration described in the enclosed product datasheet. The enzyme should be diluted appropriately with 1X PARP Buffer just before use. Note: Discard unused diluted enzyme. 5. PARP Inhibitors The 3-Aminobenzamide (3-AB) is provided at 200 mm as a control inhibitor. 3-AB will inhibit the activity of PARP at a wide range of concentrations from 2 M to 10 mm. Serially dilute the stock 3-AB and your PARP inhibitor(s) with 1X PARP Buffer and add to designated wells. 6. Strep-HRP Just before use, dilute the Strep-HRP 500-fold with 1X Strep-Diluent. A total of 50 L/well of diluted Strep-HRP is required in the assay. 4

6 PARP INHIBITOR SCREENING ASSAY PROTOCOL A. Ribosylation Reaction Note: Do not premix the PARP-HSA Enzyme and the PARP Cocktail. PARP will autoribosylate in the presence of NAD. 1. Remove excess microplate strips from the plate frame, return them to the bag containing desiccant, and reseal. Add serial dilutions of inhibitor(s) of interest previously prepared to the wells. 2. Add diluted PARP-HSA Enzyme (0.5 Unit/well) to the wells containing inhibitor. Optional: Incubate PARP and inhibitor for 10 minutes at room temperature. 3. Controls: Activity Control unit/well of PARP-HSA Enzyme without inhibitors. These wells provide the 100% activity reference point. Negative Control - A negative control without PARP should be prepared to determine background absorbance. 4. Add 25 L of 1X PARP Cocktail to each well. 5. The final reaction volume is 50 L. Volume Order of Addition Diluted test inhibitor X L 1 Diluted PARP-HSA Enzyme (0.5 unit) Y L 2 1X PARP Cocktail 25 L 3 Total volume 50 L Where X + Y = 25 L Example: If X = 10 L, make the working concentration of your inhibitor 5-fold that of the final concentration in the reaction. In this example, Y = 15 L. Therefore, dilute the PARP-HSA Enzyme to 0.5 unit/15 L. 6. Incubate the plate at room temperature for 60 minutes. The extent of ribosylation is time dependent, therefore, this step can be extended if desired. B. Detection 1. Wash the plate 4 times with 1X PBS + 0.1% Triton X-100 (200 L/well). Ensure that all the liquid is removed following each wash by inverting the plate and blotting it against clean paper towels. 2. Add 50 L of diluted Strep-HRP to each well. Incubate for 60 minutes at room temperature. 3. Wash the plate 4 times with 1X PBS + 0.1% Triton X-100 (200 L/well). Ensure that all the liquid is removed following each wash by inverting the plate and blotting it against clean paper towels. 4. Add 50 L of TACS-Sapphire to each well and incubate for minutes in the dark. TACS-Sapphire is a horseradish-peroxidase (HRP) substrate generating a soluble blue color. Color development should be monitored and the plate read at 630 nm. The reaction can be stopped by adding 50 L of 0.2 N HCl or 5% Phosphoric acid per well and the plate can then be read at 450 nm. 5

7 PARP ACTIVITY IN CELLS AND TISSUES A. Processing Cells 1. Non-Adherent Cells - Centrifuge 2 x 10 6 to 1 x 10 7 non-adherent cells at 400 x g for 10 minutes at 2-8 C. Discard the supernate. Suspend the cell pellet in 1 ml of ice cold 1X PBS and transfer to a prechilled 1.5 ml microtube. Centrifuge at 10,000 x g for 10 seconds at 2-8 C. Discard the supernate. Adherent Cells - Wash the adherent cells with 1X PBS. Cells in monolayer may be harvested by scraping in 5 ml of ice cold 1X PBS or gentle trypsinization. Transfer to a pre-chilled 15 ml tube. Centrifuge at 400 x g for 10 minutes at 2-8 C. Discard the supernate. Suspend the cell pellet in 1 ml of ice cold 1X PBS and transfer to a prechilled 1.5 ml microtube. Centrifuge at 10,000 x g for 10 seconds at 2-8 C. Discard the supernate. B. Processing Tissue 1. Remove tissue and place in cold PBS in a 50 ml conical tube. Repeatedly wash the tissue with 1X PBS to remove blood clots and other debris. 2. Transfer the tissue to a Petri dish on ice and mince the tissue into small pieces with surgical scissors. 3. Transfer the tissue pieces to a clean stainless steel sieve. Place the sieve with the tissue pieces in a Petri dish containing about 20 ml of cold 1X PBS. 4. Create a single cell suspension of the tissue as follows: Using a pestle or a round bottom tube, grind the tissue pieces thoroughly until the bulk of the tissue passes through the sieve. 5. Transfer the 1X PBS containing the single cell suspension to a 50 ml conical tube. Fill with cold 1X PBS and mix by inverting the tube several times. Let the tube stand on ice for 1 minute to allow large aggregates of tissue to settle out of solution. 6. Carefully transfer the supernate containing the single cell suspension to a clean 50 ml conical centrifuge tube. Centrifuge at 400 x g for 10 minutes at 2-8 C. Discard the supernate. Suspend the cell pellet in 1 ml of ice cold 1X PBS and transfer to a pre-chilled 1.5 ml microtube. Centrifuge at 10,000 x g for 12 seconds at 2-8 C. Discard the supernate. C. Preparation of Extracts 1. Suspend the cell pellet in 5-10 pellet volumes of cold 1X PARP Buffer containing 0.4 mm PMSF, other protease inhibitors, 0.4 M NaCl, and 1% Triton X-100 or 1% NP-40 non-ionic detergent. Incubate the cell suspensions on ice with periodic vortexing for 30 minutes. 2. Microcentrifuge the disrupted cell suspension at 10,000 x g for 10 minutes at 2-8 C to remove insoluble material. Recover the supernate to a fresh tube pre-chilled on ice. Occasionally, the pellet may float and be easily removed with a pipette tip. 3. Determine the protein concentration of the clear supernate using a Bradford or similar assay that is compatible with detergents. Use at least 20 g of protein per well in the PARP assay. 4. If samples are not used immediately, snap-freeze the clear cell extract supernates in small aliquots and store at -80 C. Avoid repeated freezing and thawing. 6

8 D. Ribosylation Reaction Note: Do not premix the cell extract and the PARP Cocktail. PARP will autoribosylate in the presence of NAD. 1. Each sample will be in 3 wells. Add X L of 1X PARP Buffer and Y L of your sample (containing at least 20 g of protein) into each of the designated 3 wells such that X + Y = 25 L. 2. Controls: PARP Standard Curve - Serially dilute the PARP-HSA Enzyme in cold microtubes with 1X PARP Buffer such that the total activity is 1 unit/25 L, 0.5 units/25 L, 0.1 units/25 L, 0.05 units/25 L, and 0.01 units/25 L. Add 25 L of each standard to triplicate wells. Negative Control - Use 25 L of 1X PARP Buffer without PARP-HSA Enzyme or cell extract as a negative control. This is included to provide the background absorbance that is subtracted from the experimental samples in the analysis of the data. 3. Add 25 L of 1X PARP Cocktail to each well. 4. Incubate the plate at room temperature for 60 minutes. The extent of ribosylation is time dependent; therefore, this step can be extended if desired. 5. The final reaction volume in each well is 50 L. Volume Order of Addition 1X PARP Buffer X L 1 Cell Extract or PARP Standard Y L 2 1X PARP Cocktail 25 L 3 Total Volume X + Y = 25 L 50 L Y = 25 L for the PARP Standards and X = 0 L X = 25 L for the Negative Control and Y = 0 L. E. Detection 1. Wash the plate 4 times with 1X PBS + 0.1% Triton X-100 (200 L/well). Ensure that all the liquid is removed following each wash by inverting the plate and blotting it against clean paper towels. 2. Add 50 L of diluted Strep-HRP to each well. Incubate for 60 minutes at room temperature. 3. Wash the plate 4 times with 1X PBS + 0.1% Triton X-100 (200 L/well). Ensure that all the liquid is removed following each wash by inverting the plate and blotting it against clean paper towels. 4. Add 50 L of TACS-Sapphire to each well and incubate for minutes in the dark. TACS-Sapphire is an HRP substrate generating a soluble blue color. Color development should be monitored and the plate read at 630 nm. The reaction can be stopped by adding 50 L of 0.2 N HCl or 5% Phosphoric acid per well and the plate can then be read at 450 nm. 7

9 DATA INTERPRETATION These curves are for demonstration only. Curves should be generated for each set of samples assayed. A. B. C. D. Figure 1: Graphical representation of the PARP standard curve and inhibition curves for 3-aminobenzamide, benzamide, and 4-amino-1,4-naphthalimide. Each point represents the median value from triplicates. 8

10 TROUBLESHOOTING GUIDE Problem Cause Solution No color in wells with inhibitor but color is present in wells with PARP alone No color in Activity Control wells No color development in wells containing cell/tissue extracts High background in wells with no PARP PARP inhibitor is extremely potent If no color develops in the wells with no inhibitor, the PARP-HSA Enzyme was not added to the wells PARP expression in cells and tissues is very low PARG activity in the extracts very is high Poor washing Increase serial dilutions of your inhibitor Add 0.5 unit of PARP-HSA Enzyme to each well Extend development time with TACS-Sapphire to 1 hour Add 1 M NaCl to a final concentration of 0.4 M in the cell extraction buffer Increase the volume and/or concentration of cell extract added to each well Add ADP-HPD (Calbiochem, Catalog # ), a specific inhibitor of PARG, to a final concentration of 100 nm Increase the number of washes with 1X PBS + Triton X-100 after the ribosylation reaction and incubation with Strep-HRP 9

11 APPENDIX Reagent Composition 1X PBS (ph 7.4) 7.5 mm disodium hydrogen phosphate (Na 2 HPO 4 ), 2.5 mm sodium dihydrogen phosphate (NaH 2 PO 4 ), 145 mm sodium chloride (NaCl) 10X Strep Diluent Biotin-reduced proprietary blocking solution 20X PARP Buffer Proprietary buffer solution 10X PARP Cocktail Proprietary solution containing biotinylated NAD PARP-HSA Enzyme PARP-HSA is provided at a concentration described in the enclosed product data sheet 3-Aminobenzamide 200 mm 3-aminobenzamide in ethanol TACS-Sapphire Peroxidase substrate readable at 630 nm (blue) or at 450 nm (yellow) after stopping the reaction with 0.2 N HCl or 5% Phosphoric acid 10X Activated DNA Activated Herring Sperm DNA in 10 mm Tris-HCl (ph 8.0), 1 mm EDTA REFERENCES 1. Satoh, M.S. and T. Lindahl (1992) Nature 356: Endres, M. et al. (1997) J. Cereb. Blood Flow Metab. 17: Eliasson, M. et al. (1997) Nat. Med. 3: Miller, M.S. et al. (1993) Soc. Neurosci. Abstr. 19: Piper, A.A. et al. (1999) Trends in Pharmacological Sciences 20: Thiemermann, C. et al. (1997) Proc. Natl. Acad. Sci. USA 94: Virag, L. and C. Szabo (2002) Pharmacological Reviews 54: Tong, W.M. et al. (2002) Cancer Res. 62: Kim, M.Y. et al. (2004) Cell 119: Curtin, N.J. (2005) Expert Rev. Mol. Med. 7:1. 10

12 NOTES TACS-Sapphire is a trademark of Trevigen, Inc. Triton X-100 is a registered trademark of The Dow Chemical Company R&D Systems, Inc /07 11